Author:
Burmeister H R,Grove M D,Peterson R E,Weisleder D,Plattner R D
Abstract
Fusarium moniliforme NRRL 13,163 produced two new fusaric acid analogs, a 10,11-dihydroxyfusaric acid and a diacid of fusaric acid in which the C-11 methyl was oxidized to a carboxyl. Several hundred milligrams of the 10,11-dihydroxyfusaric acid were routinely recovered from a kilogram of corn grit medium. It crystallized as white, irregularly shaped rectangles that melted at 153 to 154 degrees C. The diacid analog of fusaric acid crystallized as white rods that melted at 210 to 211 degrees C. Unlike the consistent recovery experienced with the 10,11-dihydroxyfusaric acid, the diacid analog proved difficult to purify after the initial discovery and was detectable in subsequent fermentations only by mass spectrometry.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference21 articles.
1. Christensen C. M. and H. H. Kaufntann. 1969. Grain storage: the role of fungi in quality loss p. 159. University of Minnesota Press Minneapolis Minn.
2. Insecticidal secondary metabolic products from the entomogenous fungus, Fusarium solani;Claydon N.;J. Invertebrate Pathol.,1977
3. Toxin from Fusarium moniliforme: effects on plants and animals;Cole R. J.;Science,1973
4. Fusaric acid as a wilt toxin;Gaumann E.;Phytopathology,1957
5. Gibberellic acid. Part V. The relation between gibberellin A, and gibberellic acid;Grove J. F.;J. Chem. Soc.,1958
Cited by
36 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献